Jellinck P H, Newcombe A M
J Steroid Biochem. 1983 Dec;19(6):1713-7. doi: 10.1016/0022-4731(83)90348-5.
Flutamide, an anti-androgen known to act through the androgen receptor, abolished the inhibitory action of testosterone on the induction of peroxidase in immature rat uteri without affecting inhibition produced by progesterone. The time course of the androgen effect on estrogen-induced uterine peroxidase, uterine weight and glucose 6-phosphate dehydrogenase activity was also determined together with the effect of flutamide on these steroid hormone-sensitive parameters. The possible mechanism of action of these compounds is discussed, particularly in the light of estrogen-induced eosinophilia. It is proposed that the observed interaction between testosterone and estradiol is mediated through their own specific receptors and not by illicit occupation of the estrogen receptor by the androgen. 5-Androstene-3 beta, 17 beta-diol (Adiol), an androgen known to exert estrogenic effects through the estrogen receptor, induced uterine peroxidase and was without significant effect on the action of estradiol, in contrast to testosterone.
氟他胺是一种已知通过雄激素受体起作用的抗雄激素药物,它消除了睾酮对未成熟大鼠子宫中过氧化物酶诱导的抑制作用,而不影响孕酮产生的抑制作用。还测定了雄激素对雌激素诱导的子宫过氧化物酶、子宫重量和葡萄糖6-磷酸脱氢酶活性的作用时间进程,以及氟他胺对这些类固醇激素敏感参数的影响。讨论了这些化合物可能的作用机制,特别是根据雌激素诱导的嗜酸性粒细胞增多现象。有人提出,观察到的睾酮和雌二醇之间的相互作用是通过它们各自的特异性受体介导的,而不是雄激素非法占据雌激素受体。5-雄烯-3β,17β-二醇(Adiol)是一种已知通过雌激素受体发挥雌激素作用的雄激素,与睾酮相反,它诱导子宫过氧化物酶,对雌二醇的作用没有显著影响。